ENST00000375128.5:c.767T>C
MANE Select
|
ENSP00000364270.5:p.Met256Thr
|
|
ENST00000375128.4:c.767T>C
|
ENSP00000364270.4:p.Met256Thr
|
|
ENST00000462523.5:c.*203T>C
|
ENSP00000433006.1:n.*203T>C
|
|
ENST00000485042.1:n.279T>C
|
|
|
NM_000380.3:c.767T>C , LRG_471t1:c.767T>C
|
NP_000371.1:p.Met256Thr
|
|
NR_027302.1:n.1115T>C
|
|
|
XM_006717278.1:c.767T>C
|
XP_006717341.1:p.Met256Thr
|
|
XM_011518988.1:c.767T>C
|
XP_011517290.1:p.Met256Thr
|
|
NM_001354975.1:c.641T>C
|
NP_001341904.1:p.Met214Thr
|
|
NR_149091.1:n.612T>C
|
|
|
NR_149092.1:n.778T>C
|
|
|
NR_149093.1:n.1304T>C
|
|
|
NR_149094.1:n.1198T>C
|
|
|
NM_000380.4:c.767T>C
MANE Select
|
NP_000371.1:p.Met256Thr
|
|
NM_001354975.2:c.641T>C
|
NP_001341904.1:p.Met214Thr
|
|
NR_027302.2:n.1046T>C
|
|
|
NR_149091.2:n.543T>C
|
|
|
NR_149092.2:n.709T>C
|
|
|
NR_149093.2:n.1235T>C
|
|
|
NR_149094.2:n.1129T>C
|
|
|